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Mutations in the P3 Protein of Soybean mosaic virus G2 Isolates Determine Virulence on Rsv4-Genotype Soybean

机译:大豆花叶病毒G2分离株P3蛋白的突变确定Rsv4-基因型大豆的毒力。

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Two Soybean mosaic virus (SMV) G2 isolates, L and L-RB, sharing high-sequence similarly but differing in ability to break Rsv4 -mediated resistance in soybean, were investigated. Infectious clones corresponding to these two isolates and their chimeric clones resulting from swapping different regions of genomic cDNA between L and L-RB were constructed. Only L-RB or chimeras containing the middle fragment of L-RB cDNA showed virulence on Rsv4 –genotype soybean. Sequence comparison analysis revealed that the middle genomic region of L and L-RB encodes four different amino acids. Point mutagenesis demonstrated that a single amino acid substitution (Q1033K) in the P3 protein determined virulence toward Rsv4 resistance. In addition, six new SMV Rsv4 resistance-breaking isolates, variants of the second passage on Williams 82 infected with the chimeras or mutants noninfectious on soybean carrying Rsv4 , were obtained. Sequencing data indicated that these new isolates contain either the Q1033K mutation or a new substitution (G1054R) in P3. Site-directed mutagenesis confirmed the virulence role of the G1054R mutation on Rsv4- genotype soybean. Taken together, these data suggest that P3 of the SMV G2 strain is an avirulent determinant for Rsv4 and one single nucleotide mutation in P3 may be sufficient to compromise its elicitor function.
机译:研究了两个大豆花叶病毒(SMV)G2分离株L和L-RB,它们具有相似的高序列,但在破坏Rsv4介导的大豆抗性上具有不同的能力。构建了与这两个分离株相对应的感染性克隆以及它们的嵌合克隆,这些嵌合克隆是由在L和L-RB之间交换基因组cDNA的不同区域产生的。只有含有L-RB cDNA中间片段的L-RB或嵌合体对Rsv4基因型大豆显示出毒力。序列比较分析显示L和L-RB的中间基因组区域编码四种不同的氨基酸。点诱变表明,P3蛋白中的单个氨基酸取代(Q1033K)确定了对Rsv4抗性的毒力。另外,获得了六种新的抗SMV Rsv4抗性分离株,即被嵌合体感染的Williams 82第二代的变体,或对携带Rsv4的大豆无感染性的突变体。测序数据表明,这些新分离株在P3中包含Q1033K突变或新取代(G1054R)。定点诱变证实了G1054R突变对Rsv4-基因型大豆的毒力作用。综上所述,这些数据表明,SMV G2菌株的P3是Rsv4的无毒决定簇,P3中的一个单核苷酸突变可能足以损害其激发子功能。

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